Evidence map›Paper›PMID 27531895›Full record

ArticleOncotarget2017

Mammalian Eps15 homology domain 1 promotes metastasis in non-small cell lung cancer by inducing epithelial-mesenchymal transition.

Qingwei Meng, Ying Xing, Tingting Ren, Hailing Lu, Yuhui Xi, Zhijun Jiang, Jing Hu, Chunhong Li, Lichun Sun, Dianjun Sun and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Qingwei MengThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Ying XingThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Tingting RenThe Sixth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Hailing LuThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Yuhui XiDepartment of Pathophysiology, Harbin Medical University, Harbin 150081, China.
Zhijun JiangDepartment of Pathophysiology, Harbin Medical University, Harbin 150081, China.
Jing HuThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Chunhong LiThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Lichun SunThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Dianjun SunThe Center for Endemic Disease Control, Chinese Center for Disease Control and Prevention, Harbin Medical University, Harbin 150081, China.
Li CaiThe Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Harbin Medical University · CNFourth Affiliated Hospital of Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CNChinese Center For Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of the earliest molecular events responsible for the metastatic dissemination of non-small cell lung cancer (NSCLC) remains critical for early detection, prevention, and treatment interventions. In this study, we hypothesized that Mammalian Eps15 homology domain 1 (EHD1) might be responsible for the metastatic behavior of cells in NSCLC. We demonstrated that upregulation of EHD1 is associated with lymph nodes metastasis and unfavorable survival in patients with NSCLC. EHD1 knockdown inhibited the invasion and migration of human NSCLC cells, and overexpression of EHD1 increased the metastatic potential of lung cancer cells. Using the Affymetrix Human Gene 1.0 ST platform, microarray analysis revealed that an association between EHD1 and epithelial-mesenchymal transition (EMT), supported by downregulation of mesenchymal markers and upregulation of epithelial markers following knockdown of EHD1 in cell lines. Moreover, overexpression of EHD1 induced the EMT and increased the metastatic potential of lung cancer cells in vitro and in vivo. These results provide a model to illustrate the relationship between EHD1 expression and lung cancer metastasis, opening up new avenues for the prognosis and therapy of lung cancer.

Indexed as

Epithelial-Mesenchymal TransitionLymphatic MetastasisAdenocarcinomaCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansMicroarray AnalysisMolecular Targeted TherapyRNA, Small InterferingSignal TransductionSurvival AnalysisVesicular Transport ProteinsEHD1 protein, humanRNA, Small InterferingVesicular Transport ProteinsEHD1epithelial-mesenchymal transitionmetastasisnon-small cell lung cancer

Identifiers

PMID27531895
PMCPMC5410234
OpenAlexW2515237737

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.